Skip to content
Study details
Enrolling now

A Phase 2 Trial Evaluating Safety and Tolerability of RCT2100

ReCode Therapeutics
NCT IDNCT06237335ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

192

Study length

about 2.9 years

Ages

18–60

Locations

13 sites in AL, AZ, CA +9

What this study is about

Researchers are testing the safety and tolerability of a new treatment, RCT2100, in healthy people and people with cystic fibrosis. The trial will involve different doses of RCT2100 administered through inhalation, either alone or with ivacaftor.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Placebo
  • 2.Take Ivacaftor
  • 3.Take RCT2100

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Oral

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

ivacaftor

Drug routes

oral (Oral Tablet)

Endpoints

Primary: Part 1: The number of participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)., Part 2: The number of participants with CF with AEs and SAEs., Part 3: The number of participants with CF with AEs and SAEs.

Body systems

Respiratory